热力学和进化在三元联体-GPCR-G蛋白质复合体中的相互作用
Hannes Junker1, Jens Meiler2, Clara T Schoeder1
1Institute for Drug Discovery, University Leipzig, Faculty of Medicine, Leipzig, Germany.
Current opinion in structural biology
|July 19, 2023
概括
G蛋白结合受体 (GPCRs) 存在于多个状态,在结合联体时产生性成本. 序列保存可能反映有约束力的合作伙伴可用性和亲和力,平衡这一成本.
科学领域:
- 生物化学 生物化学
- 分子生物学分子生物学
- 结构生物学 结构生物学
背景情况:
- G蛋白结合受体 (GPCRs) 在它们的阿波状态下表现出动态结构灵活性,其特征是高.
- 与GPCRs结合的联体减少了这种构造空间,导致信号传导过程中的代价.
- 了解形态动力学和序列保存之间的相互作用对于破译GPCR功能至关重要.
研究的目的:
- 为了研究GPCR构造动力学,配体结合和序列保存之间的关系.
- 探索结合伙伴的可用性,亲和力和结合点的刚性如何影响GPCR序列的保存.
- 讨论与GPCR介导信号传导相关的性成本.
主要方法:
- 对GPCR形态动态现有文献的分析.
- 检查各种联结体-GPCR系统中的序列保存模式.
- 由GPCRs.所采用的形状空间的划定.
主要成果:
- 在平衡状态下,GPCR填充了广泛的构成组合.
- 体受体复合体的形成导致形态的减少.
- 序列保存模式与结合伙伴特征和结合位点刚性相关.
结论:
- GPCR序列保存作为对联体结合和信号转导的能量成本的指标.
- GPCR激活的性成本是由连接体特性和受体结构特征调节的.
- 这项研究提供了对塑造GPCRs以平衡形状动态和功能要求的进化压力的见解.
相关概念视频
G-protein Coupled Receptors
120.3K
G-protein coupled receptors are ligand binding receptors that indirectly affect changes in the cell. The actual receptor is a single polypeptide that transverses the cell membrane seven times creating intracellular and extracellular loops. The extracellular loops create a ligand specific pocket which binds to neurotransmitters or hormones. The intracellular loops holds onto the G-protein.
120.3K
G Protein-coupled Receptors
12.3K
G Protein-Coupled Receptors or GPCRs are membrane-bound receptors that transiently associate with heterotrimeric G proteins and induce an appropriate response to sensory stimuli such as light, odors, hormones, cytokines, or neurotransmitters.
GPCRs are also called heptahelical, 7TM, or serpentine receptors, and consist of seven (H1-H7) transmembrane alpha-helices that span the bilayer to form a cylindrical core. The transmembrane helices are connected by three extracellular loops and three...
GPCRs are also called heptahelical, 7TM, or serpentine receptors, and consist of seven (H1-H7) transmembrane alpha-helices that span the bilayer to form a cylindrical core. The transmembrane helices are connected by three extracellular loops and three...
12.3K
Activation and Inactivation of G Proteins
7.3K
Heterotrimeric G proteins are guanine nucleotide-binding proteins. As the name suggests, heterotrimeric G proteins are composed of three subunits: alpha, beta, and gamma. They remain GDP-bound or GTP-bound inside the cells and switch between inactive/active states. The Gα subunit possesses the nucleotide-binding pocket that binds guanine nucleotides and switches between GDP or GTP-bound states. In contrast, the Gꞵ and Gγ subunits are always bound together with high...
7.3K
Transducer Mechanism: G Protein–Coupled Receptors
2.1K
G Protein–Coupled Receptors (GPCRs) are membrane-bound receptors that transiently associate with heterotrimeric G proteins and induce an appropriate response to various stimuli. GPCRs regulate critical physiological pathways and are excellent drug targets for treating diseases such as diabetes, cancer, obesity, depression, or Alzheimer's. Nearly 35% of approved drugs implement their therapeutic effects by selectively interacting with specific GPCRs.
GPCRs are also called heptahelical,...
GPCRs are also called heptahelical,...
2.1K
GPCR Desensitization
6.1K
G protein-coupled receptor (GPCR) signaling plays a crucial role in cell functioning. GPCR desensitization is an equally essential process. It allows cells to respond to changing environments and regain sensitivity to new stimuli while preventing unnecessary stimulation when no longer needed. Prolonged exposure to stimuli leads to GPCR desensitization. It involves blocking the receptors from binding and activating additional G proteins. This inhibits activation of downstream effectors, thereby...
6.1K
GPCRs Regulate Adenylyl Cylase Activity
5.7K
Some GPCRs transmit signals through adenylyl cyclase (AC), a transmembrane enzyme. AC helps synthesize second messenger cyclic adenosine monophosphate (cAMP). AC catalyzes cyclization reaction and converts ATP to cAMP by releasing a pyrophosphate. The pyrophosphate is further hydrolyzed to phosphate by the enzyme pyrophosphatase, which drives cAMP synthesis to completion. However, cAMP is rapidly degraded to 5′ AMP by the enzymes phosphodiesterase (PDE), preventing overstimulation of...
5.7K


